Synthesis of nanocrystals with variable high-index Pd facets through the controlled heteroepitaxial growth of trisoctahedral Au templates

The shape-controlled synthesis of noble metal nanocrystals (NCs) bounded by high-index facets is a current research interest because the products have the potential of significantly improving the catalytic performance of NCs in industrially important reactions. This study reports a versatile method for synthesizing polyhedral NCs enclosed by a variety of high-index Pd facets. The method is based on the heteroepitaxial growth of Pd layers on concave trisoctahedral (TOH) gold NC seeds under careful control of the growth kinetics. Polyhedral Au@Pd NCs with three different classes of high-index facets, including concave TOH NCs with {hhl} facets, concave hexoctahedral (HOH) NCs with {hkl} facets, and tetrahexahedral (THH) NCs with {hk0} facets, can be formed in high yield. The Miller indices of NCs are also modifiable, and we have used the THH NCs as a demonstrative example. The catalytic activities of these NCs were evaluated by the structure-sensitive reaction of formic acid electro-oxidation. The results showed that the high-index facets are generally more active than the low-index facets. In summary, a seeded growth process based on concave high-index faceted monometallic TOH NC templates and careful control of the growth kinetics is a simple and effective strategy for the synthesis of noble metal NCs with high-index facets. It also offers tailorability of the surface structure in shape-controlled synthesis.     

Synthesis of polyhedral iron oxide nanocrystals bound by high-index facets

High surface energy of high-index facets endows nanocrystals with high activities and thus promotes potential applications such as highly efficient catalysts,special optical,electrical and magnetic devices.But the high surface energy of the high-index facets usually drives them to grow faster than the other facets and finally disappear during the crystal growth,which leads the synthesis of nanocrystals with high-indexed facets exposed to be a great challenge.Herein,we introduced two routes to control the synthesis of-Fe2O3polyhedrons with different sets of high-index facets,one using different metal ions(Ni2+,Cu2+or Zn2+)as structure-directing agents and the other applying polymer surfactant sodium carboxymethyl cellulose(CMC)as additive.The growth process of high-index-Fe2O3polyhedrons was also discussed and possible growth mechanism was proposed.     

高指数晶面纳米催化剂的电化学制备及应用

催化剂的性能与其表面结构及组成密切相关,高指数晶面纳米晶的表面含有高密度的台阶原子等活性位点而表现出较高的催化活性. 本文综述了电化学方波电位方法用于Pt、Pd、Rh等贵金属高指数晶面结构纳米晶催化剂的制备、形成机理及其电催化性能的研究. 针对贵金属利用率问题,还着重介绍了具有较高质量活性的小粒径Pt二十四面体的制备. 在此基础上,还介绍了电化学方波电位方法用于低共熔溶剂中制备高指数晶面纳米晶,以及高指数晶面纳米催化剂的表面修饰及应用;最后对高指数晶面纳米催化剂的发展做出了展望.     

Metal ions induce growth and magnetism alternation of α-Fe2O3 crystals bound by high-index facets

In this study, quasi-cubic and hexagonal bipyramid α-Fe(2)O(3) polyhedrons with high-index facets exposed were controllably synthesized by applying metal ions Zn(2+) or Cu(2+) as structure-directing agents. The growth of the α-Fe(2)O(3) nanostructures with high-index facets were induced by metal ions without the addition of any other surfactants. The quasi-cubic form controlled by Zn(2+) looks like a cube but has an angle of approximately 86° bound by (012), (10-2), and (1-12) facets, whereas the hexagonal bipyramid form controlled by Cu(2+) has a sixfold axis bound by {012} facets. Magnetic measurements confirm that these two kinds of nanocrystals display shape- and surface-dependent magnetic behaviors. The hexagonal bipyramid iron oxide nanocrystals show a lower Morin transition temperature of 240?K and might be spin-canted ferromagnetically controlled at room temperature, and the ferromagnetism disappears at low temperature. The quasi-cubic nanocrystals have a splitting between FC curve and ZFC curve from the highest experimental temperature and no Morin transformation occurs; this indicates that they would be defect ferromagnetically controlled at low temperature. The reported metal-ion-directing technique could provide a universal method for shape- and surface-controlled synthesis of nanocrystals with high-index facets exposed.     

Electrochemical milling and faceting: size reduction and catalytic activation of palladium nanoparticles

Improved performance through milling: A method for enhancing the catalytic activity of supported metal nanoparticles is reported. This method enhances the activity for the ethanol electro-oxidation of a supported palladium catalyst. The much higher catalytic performance is ascribed to the increased electrochemically active surface area as well as the generation of high-index facets at the milled nanoparticle surface.     

Cu(2+)-assisted synthesis of hexoctahedral Au-Pd alloy nanocrystals with high-index facets

Controlled syntheses of multicomponent metal nanocrystals (NCs) and high-index surfaces have attracted increasing attention due to the specific physical and chemical properties of such NCs. Taking advantage of copper underpotential deposition as a bridge, hexoctahedral Au-Pd alloy NCs with {hkl} facets exposed were successfully synthesized, while phase separation occurred in the absence of Cu(2+) ions. The as-prepared hexoctahedral Au-Pd alloy NCs exhibited very excellent performance in terms of both formic acid electro-oxidation and methanol tolerance due to synergism between the high-index facets and the alloy.     

Electrochemically shape-controlled synthesis of trapezohedral platinum nanocrystals with high electrocatalytic activity

Trapezohedral Pt nanocrystals enclosed by 24 high-index {522} facets have been successfully prepared for the first time in high yield by a direct square wave electrodeposition method. They exhibit a significantly enhanced catalytic activity for C-1 molecules (CO, CH(3)OH, HCOOH).     

高指数晶面裸露的贵金属纳米晶体的合成

由于在高指数晶面上存在高密度的台阶位、扭结位原子等,高指数晶面裸露的贵金属纳米晶体一般表现出优越的物理化学性能,在催化、电化学等方面都有很重要的应用前景．近年来,研究人员围绕高指数晶面的制备进行了大量的工作并取得了一定进展．本文重点从合成制备方法的角度出发,结合本课题组的相关研究,系统总结了现有的有关制备高指数晶面裸露的贵金属纳米晶体的一些最新研究成果．从电化学方法、“帽”式试剂保护法、欠电位沉积原子层保护法、动力学调控、氧化刻蚀溶解再生长法以及模板法等几个方面对现有的高指数晶面裸露的贵金属纳米晶体的制备进行了总结．     

Synthesis of NiO Crystals Exposing Stable High-Index Facets

Metal oxides exposing high-index facets are potentially impactful in catalysis and adsorption processes owing to under-coordinated ions and polarities that alter their interfacial properties compared to low-index facets. Here, we report molten-salt syntheses of NiO particles exposing a variety of crystal facets. We show that for a given anion (nitrate or chloride), the alkali cation has a notable impact on the formation of crystals exposing {311}, {611}, {100}, and {111} faces. Based on a parametric analysis of synthesis conditions, we postulate that the crystallization mechanism is governed by the formation of growth units consisting of Ni^II complexes whose coordination numbers are determined by temperature and the selection of anion (associated to the coordination sphere) and alkali cation (associated with the outer coordination sphere). Notably, our findings reveal that high-index facets are particularly favored in chloride media and are stable under prolonged periods of catalysis and steaming.     

Shape-Controlled Nanocrystals for Catalytic Applications

The activity, selectivity, and long-term stability of catalyst nanoparticles can be enhanced by shape modulation. Such shaped catalytic nanocrystals have well-defined surface crystalline structures on which the cleavage and recombination of chemical bonds can be rationally controlled. Metal and metal oxide nanocrystals have been synthesized in various shapes using wet chemistry techniques such as reducing metal precursors in the presence of the surface-capping agents. The surface-capping agents should be removed prior to the catalytic chemical reaction, which necessitates clean catalytically active surface. The removal process should be performed very carefully because this removal often causes shape deformation. A few examples in which the surface-capping agents contribute positively to the chemical reactions have been reported. The examples described in this review include shaped metal, metal composite, and metal oxide nanocrystals that show enhanced catalytic activity, selectivity, and long-term stability for various gas-phase, liquid-phase, or electrocatalytic reactions. Although most of the studies using these shaped nanocrystals for catalytic applications have focused on low-index surfaces, nanocrystals with high-index facets and their catalytic applications have recently been reported. By bridging surface studies with nanoparticle catalysts using shape modulation, catalysts with improved properties can be rationally designed.     

Significantly enhancing catalytic activity of tetrahexahedral Pt nanocrystals by Bi adatom decoration

Tetrahexahedral Pt nanocrystals (THH Pt NCs) bounded by high-index facets possess a high density of active sites and display therefore a higher catalytic activity in comparison with those enclosed by low-index facets. In the current communication, we report, for the first time, the decoration of THH Pt NC surfaces by using Bi adatoms and have demonstrated that the catalytic activity of the Bi decorated THH Pt NCs toward HCOOH electrooxidation has been drastically enhanced in comparison with bare THH Pt NCs. It has also been revealed that the catalytic activity of Bi decorated THH Pt NCs for all coverages investigated always exhibits a higher catalytic activity that is about double that of Bi decorated Pt nanospheres. The study is of great importance regarding both fundamentals and applications.     

Hexoctahedral Au nanocrystals with high-index facets and their optical and surface-enhanced Raman scattering properties

Au nanocrystals (NCs) with an unprecedented hexoctahedral structure enclosed exclusively by high-index {321} facets have been prepared for the first time. Manipulating the NC growth kinetics by controlling the amount of reductant and the reaction temperature in the presence of a suitable surfactant was the key synthetic lever for controlling the morphology of the Au NCs. The hexoctahedral Au NCs exhibited efficient optical and surface-enhanced Raman scattering activities due to their unique morphological characteristics.     

Morphology-controlled synthesis of hematite nanocrystals and their facet effects on gas-sensing properties

An oriented attachment growth process was found for the morphology and shape control of various inorganic materials in solution-based systems. In this Article, a well-defined iron oxide polyhedron was prepared via a simple hydrothermal method. Detailed investigations revealed that the single-crystalline polyhedron evolved from polycrystalline aggregates. The shape and size control of the iron oxide crystals were achieved by simply adjusting the synthesis parameters. The as-prepared products exhibit excellent gas sensing selectivity to ethanol vapor. The gas-sensing ability is closely related to the exposure of high-index facets.     

Heteroepitaxial growth of high-index-faceted palladium nanoshells and their catalytic performance

The development of high-performance nanocatalysts relies essentially on the generation of stable and active surface sites at the atomic scale through synthetic control of the size, shape, and chemical composition of nanoscale metals and metal oxides. One promising route is to induce the exposure of catalytically active high-index facets of nanostructures through shape-controlled syntheses. We have designed and prepared two types of Pd nanoshells that are enclosed by high-index {730} and {221} facets through heteroepitaxial growth on high-index-faceted Au nanocrystals. The turnover numbers per surface atom of the high-index-faceted Pd nanoshells have been found to be 3-7 times those of Pd and Au-Pd core-shell nanocubes that possess only {100} facets in catalyzing the Suzuki coupling reaction. These results open up a potential for the development of inexpensive and highly active metal nanocatalysts.     

Amine-assisted synthesis of concave polyhedral platinum nanocrystals having {411} high-index facets

High-index surfaces of a face-centered cubic metal (e.g., Pd, Pt) have a high density of low-coordinated surface atoms and therefore possess enhanced catalysis activity in comparison with low-index faces. However, because of their high surface energy, the challenge of chemically preparing metal nanocrystals having high-index facets remains. We demonstrate in this work that introducing amines as the surface controller allows concave Pt nanocrystals having {411} high-index facets to be prepared through a facile wet-chemical route. The as-prepared Pt nanocrystals display a unique octapod morphology with {411} facets. The presence of high-index {411} exposed facets endows the concave Pt nanocrystals with excellent electrocatalytic activity in the oxidation of both formic acid and ethanol.     

Electroreduction of CO2 on Au(310)@Cu High-index Facets

The chemical selectivity and faradaic efficiency of high-index Cu facets for the CO₂ reduction reaction (CO₂RR) is investigated. More specifically, shape-controlled nanoparticles enclosed by Cu {hk0} facets are fabricated using Cu multilayer deposition at three distinct layer thicknesses on the surface facets of Au truncated ditetragonal nanoprisms (Au DTPs). Au DTPs are shapes enclosed by 12 high-index {310} facets. Facet angle analysis confirms DTP geometry. Elemental mapping analysis shows Cu surface layers are uniformly distributed on the Au {310} facets of the DTPs. The 7 nm Au@Cu DTPs high-index {hk0} facets exhibit a CH₄ : CO product ratio of almost 10 : 1 compared to a 1 : 1 ratio for the reference 7 nm Au@Cu nanoparticles (NPs). Operando Fourier transform infrared spectroscopy spectra disclose reactive adsorbed *CO as the main intermediate, whereas CO stripping experiments reveal the high-index facets enhance the *CO formation followed by rapid desorption or hydrogenation.     

From Gold Nanoseeds to Nanorods: The Microscopic Origin of the Anisotropic Growth

Directly manipulating and controlling the size and shape of metal nanoparticles is a key step for their tailored applications. In this work, molecular dynamics simulations were applied to understand the microscopic origin of the asymmetric growth mechanism in gold nanorods. Different factors influencing the growth were selectively included in the models to unravel the role of the surfactants and ions. In the early stage of the growth, when the seed is only a few nanometers large, a dramatic symmetry breaking occurs as the surfactant layer preferentially covers the (100) and (110) facets, leaving the (111) facets unprotected. This anisotropic surfactant layer in turn promotes anisotropic growth with the less protected tips growing faster. When silver salt is added to the growth solution, the asymmetry of the facets is preserved, but the Br^? concentration at the interface increases, resulting in increased surface passivation.     

Selective synthesis of Fe7Se8 polyhedra with exposed high-index facets and Fe7Se8 nanorods by a solvothermal process in a binary solution and their collective intrinsic properties

Fe(7)Se(8) polyhedra with high-index facets and Fe(7)Se(8) nanorods can be selectively synthesized by a solvothermal reaction in a mixed solvent of diethylenetriamine (DETA) and deionized water (DIW). It is found that the morphologies of Fe(7)Se(8) nanocrystals can be effectively controlled by adjusting the volume ratio of DETA and DIW. The unusual polyhedral crystals are bounded by two {001} and twelve {012} facets. The intrinsic properties of Fe(7)Se(8) nanocrystals have been investigated. Magnetic measurements indicate that the obtained polyhedra and nanorods show a weak ferromagnetic ordering at room temperature. In particular, a new photoluminescence emission at 403 nm from the Fe(7)Se(8) nanocrystals has been observed. The described solvothermal reaction in a mixed solvent may be extended to the synthesis of other transition-metal chalcogenide crystals with controlled shape, facets, and structure, which may bring new functionalities.     

Fabrication of Au-Pd core-shell heterostructures with systematic shape evolution using octahedral nanocrystal cores and their catalytic activity

By using octahedral gold nanocrystals with sizes of approximately 50 nm as the structure-directing cores for the overgrowth of Pd shells, Au-Pd core-shell heterostructures with systematic shape evolution can be directly synthesized. Core-shell octahedra, truncated octahedra, cuboctahedra, truncated cubes, and concave cubes were produced by progressively decreasing the amount of the gold nanocrystal solution introduced into the reaction mixture containing cetyltrimethylammonium bromide (CTAB), H(2)PdCl(4), and ascorbic acid. The core-shell structure and composition of these nanocrystals has been confirmed. Only the concave cubes are bounded by a variety of high-index facets. This may be a manifestation of the release of lattice strain with their thick shells at the corners. Formation of the [CTA](2)[PdBr(4)] complex species has been identified spectroscopically. Time-dependent UV-vis absorption spectra showed faster Pd source consumption rates in the growth of truncated cubes and concave cubes, while a much slower reduction rate was observed in the generation of octahedra. The concave cubes and octahedra were used as catalysts for a Suzuki coupling reaction. They can all serve as effective and recyclable catalysts, but the concave cubes gave higher product yields with a shorter reaction time attributed to their high-index surface facets. The concave cubes can also catalyze a wide range of Suzuki coupling reactions using aryl iodides and arylboronic acids with electron-donating and -withdrawing substituents.     

Single-Atom Rh on High-Index CeO2 Facet for Highly Enhanced Catalytic CO Oxidation

Reducible oxide-supported noble metal nanoparticles exhibit high activity in catalyzing many important oxidation reactions. However, atom migration under harsh reaction conditions leads to deactivation of the catalyst. Meanwhile, single-atom catalysts demonstrate enhanced stability, but often suffer from poor catalytic activity owing to the ionized surface states. In this work, we simultaneously address the poor activity and stability issues by synthesizing highly active and durable rhodium (Rh) single-atom catalysts through a “wrap-bake-peel” process. The pre-coated SiO₂ layer during synthesis of catalyst plays a crucial role in not only protecting CeO₂ support against sintering, but also donating electron to weaken the Ce−O bond, producing highly loaded Rh single atoms on the CeO₂ support exposed with high-index {210} facets. Benefiting from the unique electronic structure of CeO₂ {210} facets, more oxygen vacancies are generated along with the deposition of more electropositive Rh single atoms, leading to remarkably improved catalytic performance in CO oxidation.